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Evolutionary genetics of flipper forelimb and hindlimb loss from limb development-related genes in cetaceans

BACKGROUND: Cetacean hindlimbs were lost and their forelimb changed into flippers characterized by webbed digits and hyperphalangy, thus allowing them to adapt to a completely aquatic environment. However, the underlying molecular mechanism behind cetacean limb development remains poorly understood....

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Autores principales: Sun, Linxia, Rong, Xinghua, Liu, Xing, Yu, Zhenpeng, Zhang, Qian, Ren, Wenhua, Yang, Guang, Xu, Shixia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9719152/
https://www.ncbi.nlm.nih.gov/pubmed/36460960
http://dx.doi.org/10.1186/s12864-022-09024-3
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author Sun, Linxia
Rong, Xinghua
Liu, Xing
Yu, Zhenpeng
Zhang, Qian
Ren, Wenhua
Yang, Guang
Xu, Shixia
author_facet Sun, Linxia
Rong, Xinghua
Liu, Xing
Yu, Zhenpeng
Zhang, Qian
Ren, Wenhua
Yang, Guang
Xu, Shixia
author_sort Sun, Linxia
collection PubMed
description BACKGROUND: Cetacean hindlimbs were lost and their forelimb changed into flippers characterized by webbed digits and hyperphalangy, thus allowing them to adapt to a completely aquatic environment. However, the underlying molecular mechanism behind cetacean limb development remains poorly understood. RESULTS: In the present study, we explored the evolution of 16 limb-related genes and their cis-regulatory elements in cetaceans and compared them with that of other mammals. TBX5, a forelimb specific expression gene, was identified to have been under accelerated evolution in the ancestral branches of cetaceans. In addition, 32 cetacean-specific changes were examined in the SHH signaling network (SHH, PTCH1, TBX5, BMPs and SMO), within which mutations could yield webbed digits or an additional phalange. These findings thus suggest that the SHH signaling network regulates cetacean flipper formation. By contrast, the regulatory activity of the SHH gene enhancer—ZRS in cetaceans—was significantly lower than in mice, which is consistent with the cessation of SHH gene expression in the hindlimb bud during cetacean embryonic development. It was suggested that the decreased SHH activity regulated by enhancer ZRS might be one of the reasons for hindlimb degeneration in cetaceans. Interestingly, a parallel / convergent site (D42G) and a rapidly evolving CNE were identified in marine mammals in FGF10 and GREM1, respectively, and shown to be essential to restrict limb bud size; this is molecular evidence explaining the convergence of flipper-forelimb and shortening or degeneration of hindlimbs in marine mammals. CONCLUSIONS: We did evolutionary analyses of 16 limb-related genes and their cis-regulatory elements in cetaceans and compared them with those of other mammals to provide novel insights into the molecular basis of flipper forelimb and hindlimb loss in cetaceans. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-022-09024-3.
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spelling pubmed-97191522022-12-04 Evolutionary genetics of flipper forelimb and hindlimb loss from limb development-related genes in cetaceans Sun, Linxia Rong, Xinghua Liu, Xing Yu, Zhenpeng Zhang, Qian Ren, Wenhua Yang, Guang Xu, Shixia BMC Genomics Research BACKGROUND: Cetacean hindlimbs were lost and their forelimb changed into flippers characterized by webbed digits and hyperphalangy, thus allowing them to adapt to a completely aquatic environment. However, the underlying molecular mechanism behind cetacean limb development remains poorly understood. RESULTS: In the present study, we explored the evolution of 16 limb-related genes and their cis-regulatory elements in cetaceans and compared them with that of other mammals. TBX5, a forelimb specific expression gene, was identified to have been under accelerated evolution in the ancestral branches of cetaceans. In addition, 32 cetacean-specific changes were examined in the SHH signaling network (SHH, PTCH1, TBX5, BMPs and SMO), within which mutations could yield webbed digits or an additional phalange. These findings thus suggest that the SHH signaling network regulates cetacean flipper formation. By contrast, the regulatory activity of the SHH gene enhancer—ZRS in cetaceans—was significantly lower than in mice, which is consistent with the cessation of SHH gene expression in the hindlimb bud during cetacean embryonic development. It was suggested that the decreased SHH activity regulated by enhancer ZRS might be one of the reasons for hindlimb degeneration in cetaceans. Interestingly, a parallel / convergent site (D42G) and a rapidly evolving CNE were identified in marine mammals in FGF10 and GREM1, respectively, and shown to be essential to restrict limb bud size; this is molecular evidence explaining the convergence of flipper-forelimb and shortening or degeneration of hindlimbs in marine mammals. CONCLUSIONS: We did evolutionary analyses of 16 limb-related genes and their cis-regulatory elements in cetaceans and compared them with those of other mammals to provide novel insights into the molecular basis of flipper forelimb and hindlimb loss in cetaceans. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-022-09024-3. BioMed Central 2022-12-02 /pmc/articles/PMC9719152/ /pubmed/36460960 http://dx.doi.org/10.1186/s12864-022-09024-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Sun, Linxia
Rong, Xinghua
Liu, Xing
Yu, Zhenpeng
Zhang, Qian
Ren, Wenhua
Yang, Guang
Xu, Shixia
Evolutionary genetics of flipper forelimb and hindlimb loss from limb development-related genes in cetaceans
title Evolutionary genetics of flipper forelimb and hindlimb loss from limb development-related genes in cetaceans
title_full Evolutionary genetics of flipper forelimb and hindlimb loss from limb development-related genes in cetaceans
title_fullStr Evolutionary genetics of flipper forelimb and hindlimb loss from limb development-related genes in cetaceans
title_full_unstemmed Evolutionary genetics of flipper forelimb and hindlimb loss from limb development-related genes in cetaceans
title_short Evolutionary genetics of flipper forelimb and hindlimb loss from limb development-related genes in cetaceans
title_sort evolutionary genetics of flipper forelimb and hindlimb loss from limb development-related genes in cetaceans
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9719152/
https://www.ncbi.nlm.nih.gov/pubmed/36460960
http://dx.doi.org/10.1186/s12864-022-09024-3
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